Gene Symbol | Mmp21 |
Entrez Gene ID | 293573 |
Full Name | matrix metallopeptidase 21 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
ORF » Species Summary » Rattus norvegicus » Mmp21 cDNA ORF clone
Gene Symbol | Mmp21 |
Entrez Gene ID | 293573 |
Full Name | matrix metallopeptidase 21 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
mRNA | Protein | Name |
---|---|---|
NM_001106308.1 | NP_001099778.1 | matrix metalloproteinase-21 precursor |
Pan troglodytes (chimpanzee) | MMP21 | XP_003312866.1 |
MMP21 | XP_001085506.1 | |
Danio rerio (zebrafish) | LOC100003089 | XP_001342721.4 |
Rattus norvegicus (Norway rat) | Mmp21 | NP_001099778.1 |
Xenopus tropicalis (tropical clawed frog) | mmp21 | XP_002932698.2 |
Homo sapiens (human) | MMP21 | NP_671724.1 |
Mus musculus (house mouse) | Mmp21 | NP_694423.1 |
Canis lupus familiaris (dog) | MMP21 | XP_003640036.1 |
A human laterality disorder caused by a homozygous deleterious mutation in MMP21.
Perles Z, Moon S, Ta-Shma A, Yaacov B, Francescatto L, Edvardson S, Rein AJ, Elpeleg O, Katsanis N
Journal of medical genetics52(12)840-7(2015 Dec)
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Guimier A, Gabriel GC, Bajolle F, Tsang M, Liu H, Noll A, Schwartz M, El Malti R, Smith LD, Klena NT, Jimenez G, Miller NA, Oufadem M, Moreau de Bellaing A, Yagi H, Saunders CJ, Baker CN, Di Filippo S, Peterson KA, Thiffault I, Bole-Feysot C, Cooley LD, Farrow EG, Masson C, Schoen P, Deleuze JF, Nitschk? P, Lyonnet S, de Pontual L, Murray SA, Bonnet D, Kingsmore SF, Amiel J, Bouvagnet P, Lo CW, Gordon CT
Nature genetics47(11)1260-3(2015 Nov)
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Li Y, Klena NT, Gabriel GC, Liu X, Kim AJ, Lemke K, Chen Y, Chatterjee B, Devine W, Damerla RR, Chang C, Yagi H, San Agustin JT, Thahir M, Anderton S, Lawhead C, Vescovi A, Pratt H, Morgan J, Haynes L, Smith CL, Eppig JT, Reinholdt L, Francis R, Leatherbury L, Ganapathiraju MK, Tobita K, Pazour GJ, Lo CW
Nature521(7553)520-4(2015 May)
Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7.
Nagamachi A, Matsui H, Asou H, Ozaki Y, Aki D, Kanai A, Takubo K, Suda T, Nakamura T, Wolff L, Honda H, Inaba T
Cancer cell24(3)305-17(2013 Sep)
Matrix metalloproteinase-21 expression is associated with keratinocyte differentiation and upregulated by retinoic acid in HaCaT cells.
Skoog T, Elomaa O, Pasonen-Sepp?nen SM, Forsberg S, Ahokas K, Jeskanen L, P?rssinen J, Tiala I, Rollman O, Lohi J, Saarialho-Kere U
The Journal of investigative dermatology129(1)119-30(2009 Jan)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
MMP-21 may be an important protease in the terminal differentiation of keratinocytes
Title: Matrix metalloproteinase-21 expression is associated with keratinocyte differentiation and upregulated by retinoic acid in HaCaT cells.
The following Mmp21 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Mmp21 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
CloneID | ORa00839 | |
Clone ID Related Accession (Same CDS sequence) | NM_001106308.1 | |
Accession Version | NM_001106308.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 1707bp) Protein sequence SNP |
|
Vector | pcDNA3.1-C-(k)DYK or customized vector | User Manual |
Clone information | Clone Map | MSDS |
Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
ORF Insert Method | CloneEZ™ Seamless cloning technology | |
Insert Structure | linear | |
Update Date | 2017-10-01 | |
Organism | Rattus norvegicus(Norway rat) | |
Product | matrix metalloproteinase-21 precursor | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from CH473953.1. On or before Oct 4, 2007 this sequence version replaced XM_001054903.1, XM_219415.4. ##Evidence-Data-START## RNAseq introns :: mixed/partial sample support SAMD00052297, SAMEA2689602 [ECO:0000350] ##Evidence-Data-END## |
1 | ATGCTTGCTG TCTCTGACTT GCGTCTGACA ATGCTGCTCT GCTGGCTAGT TACACCCCAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001099778.1 |
CDS | 16..1722 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001106308.1 |
1 | ATGCTTGCTG TCTCTGACTT GCGTCTGACA ATGCTGCTCT GCTGGCTAGT TACACCCCAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
A human laterality disorder caused by a homozygous deleterious mutation in MMP21. |
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. |
Global genetic analysis in mice unveils central role for cilia in congenital heart disease. |
Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7. |
Matrix metalloproteinase-21 expression is associated with keratinocyte differentiation and upregulated by retinoic acid in HaCaT cells. |